196 English-speaking jobs in Walloon Brabant

Senior SAP PP Consultant supports customers in optimizing production and manufacturing processes. Designs, configures, and implements SAP S/4HANA PP solutions. Collaborates with customers and project teams to ensure successful project delivery. Requires 3+ years of experience as a SAP PP Consultant with strong S/4HANA expertise.

Senior SAP PP Consultant supports customers in optimizing production and manufacturing processes. Designs, configures, and implements SAP S/4HANA PP solutions. Collaborates with customers and project teams to ensure successful project delivery. Requires minimum 3 years of experience as a SAP PP Consultant with strong expertise in S/4HANA environments.

Technical Writer will create, structure, and maintain technical documentation for complex medical devices. Responsibilities include developing user guides, collaborating with engineering teams, and translating technical concepts into clear, accessible language. Requires a Master's degree in a relevant field and 3+ years of technical writing experience.

Amaris Consulting seeks a DT Technical Lead to drive the evolution and deployment of critical laboratory systems for a leading client. This role involves leading technical solutions, translating business needs into technical designs, and ensuring regulatory compliance in a GxP environment.

Senior Solution Consultant needed with a university degree in engineering, business engineering, computer science, or a related field. Strong programming skills, including macro coding, are required. Excellent analytical and communication skills are essential.

Azure Cloud Architect needed with 6+ years of experience in cloud engineering, architecture, or DevOps. Expertise in Microsoft Azure, Kubernetes, Terraform, Docker, and CI/CD pipelines required.

Solution Consultant needed with a university degree in engineering, business engineering, computer science, or a related field. Strong programming skills, including macro coding, are required. Excellent analytical and communication skills are essential.

Account Manager with 10+ years of experience in supply chain software solutions for manufacturing companies. Proven ability to build trust with senior management and articulate viewpoints effectively. Experience with CRM solutions like Salesforce.com.

Senior Scientist to design, develop, and optimize injectable drug product manufacturing processes for clinical and late-stage development. Requires advanced degree and 8+ years experience in sterile liquid injectable drug product development or manufacturing.

Digital Solutions Architect will shape and deliver the digital transformation of the Patient Supply organization. You will develop technology roadmaps, architectures, and solutions, focusing on a next-generation biologics facility. You will work with global technology and business leaders to drive large-scale transformation programs.

The Impact Quality Lead ensures pharmacovigilance activities comply with global regulatory requirements, guidelines, policies, and industry best practices. This role provides oversight to Phase IV studies, post-marketing commitments, and patient-centric initiatives. Responsibilities include supporting the pharmacovigilance system, managing SOPs and training, and partnering with vendors. The Impact Quality Lead also monitors compliance, conducts audits, and manages deviations and risks.

Leads a global quality team supporting operational and strategic activities for Suppliers & Materials Quality Management. Oversees the implementation and continuous enhancement of qualification processes, ensuring alignment with regulatory requirements and internal policies. Drives global harmonization and standardization of the supplier qualification lifecycle and material quality oversight.

Operational QA to support product and process quality within a pharmaceutical site. Responsibilities include drafting, reviewing, and analyzing data for PQRs. Requires a Master's degree or equivalent in a scientific field and 2-4 years of experience in pharmaceutical quality.

Provides global Quality oversight for Network Governance across Patient Supply Third-Party partners, Inspection Readiness, and Regulatory Intelligence. Ensures Third-Party lifecycle management, governance decisions, and inspection-related activities meet UCB quality standards. Leads Quality oversight for Network Governance and embeds Quality across Third-Party lifecycle processes. Manages and coaches the Inspection Readiness Quality Support function. Coordinates Regulatory Information Notifications and ensures timely SME evaluation and implementation. Represents Quality in governance bodies and escalates risks impacting compliance or supply.

Lead discovery-stage process development and analytical innovation for a lentiviral vector platform. Design, optimize, and characterize processes for small-scale bioreactor manufacturing. Collaborate with cross-functional teams to ensure alignment and tech-transfer readiness.

Leads global sales vision and strategy for IBA's Industrial Business Unit. Develops and executes commercial roadmaps, talent acquisition, and sales processes. Manages an international team of 10 sales professionals. Requires 15+ years of international industrial sales experience, proven strategy development, and people management skills.

Technology Scout to identify, evaluate, and lead maturation of emerging technologies in nuclear energy. Will bridge the gap between advancements and business applications, leading technology partnership/expansion efforts.

The Oncology Pipeline MSL is a field-based role connecting GSK to the healthcare community. This non-promotional position focuses on advancing clinical practice to improve patient outcomes. The MSL engages with healthcare providers and account personnel to ensure understanding of GSK medicines, their benefit/risk profile, and the evolving treatment landscape. Responsibilities include identifying and engaging with healthcare professionals, contributing to medical strategy by collecting and communicating medical insights, and supporting clinical trials.

The Evidence Quality Lead ensures compliant Research, Development and Pharmacovigilance processes from candidate to commercial branding. This role develops and maintains quality strategies, identifies and manages risks, and leads compliance investigations. The ideal candidate has a Bachelor's degree in a relevant field, 10+ years in the (bio)pharmaceutical industry, and experience in GLP, GCP, and/or GVP quality auditing.

Verbolia seeks a Senior Technical Product Manager to lead product initiatives for its SEO/GEO platform. You will translate customer needs into product requirements, collaborate with engineering, and drive execution of scalable solutions. 3+ years of experience as a Technical Product Manager is required, along with a passion for AI and a strong technical background.